TY - JOUR
T1 - Platinum nanoparticles-loaded holey reduced graphene oxide framework as freestanding counter electrodes of dye sensitized solar cells and methanol oxidation catalysts
AU - Yu, Mei
AU - Wu, Xueke
AU - Zhang, Jindan
AU - Meng, Yanbing
AU - Ma, Yuxiao
AU - Liu, Jianhua
AU - Li, Songmei
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/12/20
Y1 - 2017/12/20
N2 - Platinum nanoparticles (PtNPs)-loaded holey reduced graphene oxide framework (Pt/HGF) has been synthesized as freestanding counter electrodes (CEs) of dye sensitized solar cells (DSSCs) and methanol oxidation catalysts. PtNPs (∼2.5 nm) are uniformly incorporated into holey reduced graphene oxide framework by a solvothermal treatment. Pt/HGF possesses high specific surface area (340.65 m2 g−1). Its charge transfer resistance (RCT) at the I−/I3− electrolyte/CE interface reaches 1.61 Ω cm2, lower than that of pure Pt (2.99 Ω cm2) and PtNPs loaded non-hole reduced graphene oxide (Pt/G, 2.37 Ω cm2), and its RCT at the methanol electrolyte/electrode interface (0.75 Ω cm2) is much lower than that of Pt/G (3.14 Ω cm2), showing good electrocatalytic activity for I−/I3− redox reaction and methanol oxidation reaction (MOR). The assembled Pt/HGF-DSSC achieves a photoelectric conversion efficiency of 5.55% and a short-circuit current density (Jsc) of 12.27 mA cm−2, better than those of Pt-DSSC (5.19%, 10.50 mA cm−2) and Pt/G-DSSC (5.12%, 11.12 mA cm−2). In methanol oxidation test, Pt/HGF delivers better electrocatalytic activity and stability than Pt/G. Thus, high electrocatalytic activity and efficient electron/ion transport are achieved by Pt/HGF due to the synergistic effect of well dispersed PtNPs, hierarchical holey structure, and framework, and it may serve as an alternative of pure Pt for DSSC-CEs and MOR catalysts.
AB - Platinum nanoparticles (PtNPs)-loaded holey reduced graphene oxide framework (Pt/HGF) has been synthesized as freestanding counter electrodes (CEs) of dye sensitized solar cells (DSSCs) and methanol oxidation catalysts. PtNPs (∼2.5 nm) are uniformly incorporated into holey reduced graphene oxide framework by a solvothermal treatment. Pt/HGF possesses high specific surface area (340.65 m2 g−1). Its charge transfer resistance (RCT) at the I−/I3− electrolyte/CE interface reaches 1.61 Ω cm2, lower than that of pure Pt (2.99 Ω cm2) and PtNPs loaded non-hole reduced graphene oxide (Pt/G, 2.37 Ω cm2), and its RCT at the methanol electrolyte/electrode interface (0.75 Ω cm2) is much lower than that of Pt/G (3.14 Ω cm2), showing good electrocatalytic activity for I−/I3− redox reaction and methanol oxidation reaction (MOR). The assembled Pt/HGF-DSSC achieves a photoelectric conversion efficiency of 5.55% and a short-circuit current density (Jsc) of 12.27 mA cm−2, better than those of Pt-DSSC (5.19%, 10.50 mA cm−2) and Pt/G-DSSC (5.12%, 11.12 mA cm−2). In methanol oxidation test, Pt/HGF delivers better electrocatalytic activity and stability than Pt/G. Thus, high electrocatalytic activity and efficient electron/ion transport are achieved by Pt/HGF due to the synergistic effect of well dispersed PtNPs, hierarchical holey structure, and framework, and it may serve as an alternative of pure Pt for DSSC-CEs and MOR catalysts.
KW - Dye sensitized solar cells
KW - Freestanding counter electrodes
KW - Holey reduced graphene oxide framework
KW - Methanol oxidation catalysts
KW - Platinum nanoparticles
UR - https://www.scopus.com/pages/publications/85035229003
U2 - 10.1016/j.electacta.2017.11.086
DO - 10.1016/j.electacta.2017.11.086
M3 - 文章
AN - SCOPUS:85035229003
SN - 0013-4686
VL - 258
SP - 485
EP - 494
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -